Clinical Haematology, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, 305 Grattan St, Melbourne, VIC, 3000, Australia.
Department of Infectious Diseases, Peter MacCallum Cancer Centre, Melbourne, Australia.
Ann Hematol. 2024 Feb;103(2):593-602. doi: 10.1007/s00277-023-05526-6. Epub 2023 Nov 6.
Infectious diarrhoea is common post-allogeneic haematopoietic stem-cell transplantation (alloHSCT). While the epidemiology of Clostridioides difficile infection (CDI) post-alloHSCT has been described, the impact of other diarrhoeal pathogens is uncertain. We reviewed all alloHSCT between 2017 and 2022 at a single large transplant centre; 374 patients were identified and included. The 1-year incidence of infectious diarrhoea was 23%, divided into viral (13/374, 3%), CDI (65/374, 17%) and other bacterial infections (16/374, 4%). There was a significant association between infectious diarrhoea within 1 year post-transplant and the occurrence of severe acute lower gastrointestinal graft-versus-host disease (GVHD, OR = 4.64, 95% CI 2.57-8.38, p < 0.001) and inferior GVHD-free, relapse-free survival on analysis adjusted for age, donor type, stem cell source and T-cell depletion (aHR = 1.64, 95% CI = 1.18-2.27, p = 0.003). When the classes of infectious diarrhoea were compared to no infection, bacterial (OR = 6.38, 95% CI 1.90-21.40, p = 0.003), CDI (OR = 3.80, 95% CI 1.91-7.53, p < 0.001) and multiple infections (OR = 11.16, 95% CI 2.84-43.92, p < 0.001) were all independently associated with a higher risk of severe GI GVHD. Conversely, viral infections were not (OR = 2.98, 95% CI 0.57-15.43, p = 0.20). Non-viral infectious diarrhoea is significantly associated with the development of GVHD. Research to examine whether the prevention of infectious diarrhoea via infection control measures or modulation of the microbiome reduces the incidence of GVHD is needed.
异基因造血干细胞移植(alloHSCT)后常发生感染性腹泻。虽然 alloHSCT 后艰难梭菌感染(CDI)的流行病学已有描述,但其他腹泻病原体的影响尚不确定。我们回顾了单一大型移植中心 2017 年至 2022 年间所有 alloHSCT;共确定并纳入 374 例患者。感染性腹泻的 1 年发生率为 23%,分为病毒性(13/374,3%)、CDI(65/374,17%)和其他细菌感染(16/374,4%)。移植后 1 年内发生感染性腹泻与严重急性下胃肠道移植物抗宿主病(GVHD,OR=4.64,95%CI 2.57-8.38,p<0.001)的发生以及年龄、供体类型、干细胞来源和 T 细胞耗竭调整后的无严重 GVHD、无复发生存的不良预后显著相关(aHR=1.64,95%CI 1.18-2.27,p=0.003)。当将感染性腹泻的类型与无感染、细菌(OR=6.38,95%CI 1.90-21.40,p=0.003)、CDI(OR=3.80,95%CI 1.91-7.53,p<0.001)和多重感染(OR=11.16,95%CI 2.84-43.92,p<0.001)进行比较时,它们都与严重胃肠道 GVHD 的风险增加独立相关。相反,病毒感染则不然(OR=2.98,95%CI 0.57-15.43,p=0.20)。非病毒性感染性腹泻与 GVHD 的发生显著相关。需要研究通过感染控制措施或微生物组调节来预防感染性腹泻是否能降低 GVHD 的发生率。